Efficacy of Platinum/Pemetrexed Combination Chemotherapy in ALK-Positive NSCLC Refractory to Second-Generation ALK Inhibitors

被引:64
作者
Lin, Jessica J. [1 ]
Schoenfeld, Adam J. [2 ]
Zhu, Viola W. [3 ]
Yeap, Beow Y. [1 ]
Chin, Emily [1 ]
Rooney, Marguerite [1 ]
Plodkowski, Andrew J. [4 ]
Digumarthy, Subba R. [5 ]
Dagogo-Jack, Ibiayi [1 ]
Gainor, Justin F. [1 ]
Ou, Sai-Hong Ignatius [3 ]
Riely, Gregory J. [2 ]
Shaw, Alice T. [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[3] Univ Calif Irvine, Sch Med, Chao Family Comprehens Canc Ctr, Orange, CA 92668 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10021 USA
[5] Massachusetts Gen Hosp, Dept Radiol, Boston, MA USA
关键词
Chemotherapy; Efficacy; ALK; NSCLC; OPEN-LABEL; CRIZOTINIB; PROGRESSION; ALECTINIB;
D O I
10.1016/j.jtho.2019.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The current standard initial therapy for advanced ALK receptor tyrosine kinase (ALK)-positive NSCLC is a second-generation ALK tyrosine kinase inhibitor (TKI) such as alectinib. The optimal next-line therapy after failure of a second-generation ALK TKI remains to be established; however, standard options include the third-generation ALK TKI lorlatinib or platinum/pemetrexedbased chemotherapy. The efficacy of platinum/pemetrexed-based chemotherapy has not been evaluated in cases that are refractory to second-generation TKIs. Methods: This was a retrospective study performed at three institutions. Patients were eligible if they had advanced ALK-positive NSCLC refractory to one or more second-generation ALK TKI(s) and had received platinum/pemetrexed-based chemotherapy. Results: Among 58 patients eligible for this study, 37 had scans evaluable for response with measurable disease at baseline. The confirmed objective response rate to platinum/pemetrexed-based chemotherapy was 29.7% (11 of 37 patients; 95% confidence interval [CI]: 15.9% - 47.0%), with median duration of response of 6.4 months (95% CI: 1.6 months - not reached). The median progression-free survival for the entire cohort was 4.3 months (95% CI: 2.9 - 5.8 months). Progression-free survival was longer in patients who received platinum/pemetrexed in combination with an ALK TKI compared to those who received platinum/pemetrexed alone (6.8 months vs. 3.2 months, respectively; hazard ratio = 0.33; p = 0.025). Conclusions: Platinum/pemetrexed-based chemotherapy shows modest efficacy in ALK-positive NSCLC after failure of second-generation ALK TKIs. The activity may be higher if administered with an ALK TKI, suggesting a potential role for continued ALK inhibition. (C) 2019 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:258 / 265
页数:8
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